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US6063811A - Compositions for a once day treatment of cyclooxygenase-2 mediated diseases - Google Patents

Compositions for a once day treatment of cyclooxygenase-2 mediated diseases Download PDF

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Publication number
US6063811A
US6063811A US09/180,647 US18064799A US6063811A US 6063811 A US6063811 A US 6063811A US 18064799 A US18064799 A US 18064799A US 6063811 A US6063811 A US 6063811A
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US
United States
Prior art keywords
phenyl
treatment
cyclooxygenase
methylsulfonyl
furanone
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US09/180,647
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English (en)
Inventor
Bruno Hancock
Conrad Winters
Barry Gertz
Elliot Ehrich
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Frosst Canada and Co
Merck Sharp and Dohme LLC
Original Assignee
Merck Frosst Canada and Co
Merck and Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Priority claimed from GBGB9612063.9A external-priority patent/GB9612063D0/en
Priority to US09/180,647 priority Critical patent/US6063811A/en
Application filed by Merck Frosst Canada and Co, Merck and Co Inc filed Critical Merck Frosst Canada and Co
Assigned to MERCK FROSST CANADA & CO. reassignment MERCK FROSST CANADA & CO. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WINTERS, CONRAD, HANCOCK, BRUNO
Assigned to MERCK & CO., INC. reassignment MERCK & CO., INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GERTZ, BARRY, EHRICH, ELLIOT
Publication of US6063811A publication Critical patent/US6063811A/en
Application granted granted Critical
Assigned to MERCK FROSST CANADA AND COMPANY reassignment MERCK FROSST CANADA AND COMPANY CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: MERCK FROSST CANADA, INC.
Assigned to MERCK FROSST COMPANY reassignment MERCK FROSST COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MERCK FROSST CANADA AND COMPANY
Assigned to MERCK SHARP & DOHME CORP. reassignment MERCK SHARP & DOHME CORP. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: MERCK & CO., INC.
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365—Lactones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Definitions

  • This invention relates to pharmaceutical compositions for the treatment of cyclooxygenase-2 mediated diseases, mehe use of a compound in the manufacture of a medicament.
  • this invention relates to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, said composition being suitable for once a day administration, said composition comprising a cyclooxygenase-2 inhibiting characterized by high potency for the inhibition of cyclooxygenase-2, a long half-life and a high degree of specificity for inhibiting cyclooxygenase-2 in preference to cyclooxygenase-1.
  • a compound is exemplified by 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone, ##STR1##
  • Non-steroidal anti-inflammatory agents are normally administered 2 to 4 times daily.
  • the relatively short half-life of most non-steroidal anti-inflammatory agents means that once a day administration is impractical and even twice a day administration is unusual.
  • the relatively large doses needed to achieve once a day treatment of conventional non-steroidal anti-inflammatory agents would also lead to side effects so that there is a general understanding that once a day administration is unlikely to be achievable.
  • active agent possesses a half-life in humans of sufficient length that a single oral dose of 5 to 125 mg of agent per day will provide effective safe anti-inflammatory treatment over a 24 hour period.
  • active agents are particularly useful in the treatment of chronic indications, including arthritis, pain, Alzheimer's disease and the like.
  • This invention is directed to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, said composition being suitable for once a day oral administration, said composition comprising a cyclooxygenase-2 inhibiting compound characterized by high potency for the inhibition of cyclooxygenase-2, a long half-life and a high degree of specificity for inhibiting cyclooxygenase-2 in preference to cyclooxygenase-1.
  • a cyclooxygenase-2 inhibiting compound characterized by high potency for the inhibition of cyclooxygenase-2, a long half-life and a high degree of specificity for inhibiting cyclooxygenase-2 in preference to cyclooxygenase-1.
  • Such a compound is exemplified by 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone.
  • this invention is directed to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, aid composition being suitable for once a day oral administration, said composition comprising 5 to 125 mgs of the above mentioned compound.
  • the invention is also directed to a method of treating cyclooxygenase-2 mediated diseases comprising the once a day oral administration of 5 to 125 mgs of the above mentioned compound.
  • the invention is also directed to the use the above mentioned compound in the manufacture of a medicament containing 5 to 125 mgs of said compound for once a day administration for the treatment of cyclooxygenase-2 mediated diseases.
  • this invention is directed to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, said composition being suitable for once a day administration, said composition comprising a cyclooxygenase-2 inhibitor characterized by high potency for the inhibition of cyclooxygenase-2, a long half-life and a high degree of specificity for inhibiting cyclooxygenase-2 in preference to cyclooxygenase-1.
  • this invention is directed to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, said composition being suitable for once a day oral administration, said composition comprising a cyclooxygenase-2 inhibiting compound characterized by.
  • this invention is directed only to compounds which act by inhibiting cyclooxygenase-2.
  • the characterization requirements set out above cannot be said to be met unless the mode of action of the compound is as an inhibitor of cyclooxygenase-2.
  • a central nervous system agent may relieve pain with a potency equal to or greater than ibuprofen, yet not meet the requirements set out above, because it does not act on cyclooxygenase-2. See Inflamm. Res.
  • this invention is directed to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, said composition being suitable for once a day oral administration, said composition comprising a 5 to 125 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone, and a pharmaceutical carrier therefor.
  • such a compound may inhibit cellular neoplastic transformations and metastic tumor growth and hence can be used in the treatment of cancer. It is also useful for the treatment of dementia including pre-senile and senile dementia, and in particular, dementia associated with Alzheimer Disease (ie Alzheimer's dementia).
  • the compound will also inhibit prostanoid-induced smooth muscle contraction by preventing the synthesis of contractile prostanoids and hence may be of use in the treatment of dysmenorrhea, premature labor and asthma.
  • the specified compound is also useful as an alternative to conventional non-steroidal antiinflammatory drugs (NSAID'S) particularly where such NSAIDS may be contra-indicated such as in patients with peptic ulcers, gastritis, regional enteritis, ulcerative colitis, diverticulitis or with a recurrent history of gastrointestinal lesions; GI bleeding, coagulation disorders including anemia such as hypoprothrombinemia, haemophilia or other bleeding problems (including those relating to reduced or impaired platelet function); kidney disease (eg impaired renal function); those prior to surgery or taking anticoagulants; and those susceptible to NSAID induced asthma.
  • NSAID'S non-steroidal antiinflammatory drugs
  • the compound may be administered orally or by intravenous infusion.
  • compositions for treating COX-2 mediated diseases as defined may optionally include one or more ingredients as listed above.
  • compositions containing the active ingredient may be in a form suitable for oral use, for example, as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs.
  • the compositions are intended for oral use and may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions and such compositions may contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide pharmaceutically elegant and palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets.
  • excipients may be for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example starch, gelatin or acacia, and lubricating agents, for example, magnesium stearate, stearic acid or talc.
  • inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate
  • granulating and disintegrating agents for example, corn starch, or alginic acid
  • binding agents for example starch, gelatin or acacia
  • lubricating agents for example, magnesium stearate, stearic acid or talc.
  • 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone to possess a surprising combination of attributes. Not only are these active agents potent safe and effective at modest oral dosages of 5 to 125 mg of agent per day, but in addition these active agents possess a half-life in humans of sufficient length that a single oral dose of 5 to 125 mg of active agent per day will provide effective safe anti-inflammatory treatment over a 24 hour period. Such agents are particularly useful in the treatment of chronic indications, such as rheumatoid and osteo arthritis as well as Alzheimer's Disease.
  • Oral and intravenous dosage levels for agent 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone are of the order of from about 5 to 125 per patient per day.
  • the amount of active agent that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
  • a formulation intended for the oral administration of humans may contain from 5 to 125 mg of agent compounded with an appropriate and convenient amount of carrier material which may vary from about 5 to about 95 percent of the total composition.
  • Dosage unit forms may typically contain 5, 10, 12.5, 20, 25, 50, 75, 100 or 125 mg of active agent.
  • the specific dose level for any particular patient will depend upon a variety of factors including the age, body weight, general health, sex, diet, time of administration, rate of excretion, drug combination and the type and severity of the particular disease undergoing therapy. For many patients, a dosage range of 5 to 50 or 12.5 to 25 or 25 to 75 mg per day is preferred.
  • a dosage of 5 to 50 or 12.5 to 25 mg per day is preferred. More particularly, for the treatment of osteoarthritis, a dosage of 5, 10, 12.5, 25 or 50 mg per day is preferred, whereas for the treatment of rheumatoid arthritis, 10, 12.5, 25 or 50 mg per day is preferred.
  • a dosage of 5 to 50 or 12.5 to 25 mg per day is preferred. More particularly, for the treatment of osteoarthritis, a dosage of 5, 10, 12.5, 25 or 50 mg per day is preferred, whereas for the treatment of rheumatoid arthritis, 10, 12.5, 25 or 50 mg per day is preferred.
  • non-chronic indications such as headache or post-operative swelling and pain, 10, 12.5, 25 or 50 mg per day is preferred.
  • the invention is directed to a unit dose oral form which comprises from 5 to 50 or 5 to 22.5 mg of the cyclooxygenase inhibitor, for example, 12.5 or 20 mg or 12.5 to 25.
  • this invention is directed to a pharmaceutical composition for the treatment of cyclooxygenase-2 mediated diseases, said composition suitable for once a day oral administration, said composition comprising a 5 to 50 or 25 to 75 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone, and a pharmaceutical carried therefor.
  • compositions comprising 5 to 50 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone.
  • compositions comprising 10 to 50 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone.
  • compositions comprising 5 to 22.5 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone.
  • compositions comprising 12.5 to 25 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone.
  • compositions comprising 5, 10, 12.5, 25 or 50 mg of 3-phenyl-4-(4-methylsulfonyl)phenyl)-2-(5H)-furanone.
  • Tablet dose strengths of between 5 and 125 mg can be accomodated by varying total tablet weight, and the ratio of the first three ingredients. Generally it is preferable to maintain a 1:1 ratio for microcrystalline cellulose: lactose monohydrate.
  • Tablet dose strengths of between 5 and 125 mg can be accomodated by varying total tablet weight, and the ratio of the first three ingredients. Generally it is preferable to maintain a 1:1 ratio for microcrystalline cellulose: lactose monohydrate.
  • Capsule dose strengths of between 1 and 50 mg can be accomodated by varying total fill weight, and the ratio of the first three ingredients. Generally it is preferable to maintain a 1:1 ratio for microcrystalline cellulose: lactose monohydrate.
  • Solution dose strengths of between 1 and 50 mg/5 mL can be accomodated by varying the ratio of the two ingredients.
  • Suspension dose strengths of between 1 and 50 mg/5 ml can be accomodated by varying the ratio of the first two ingredients.
  • Step 1 To a solution of phenylacetic acid (27.4 g, 201 mmol) and 2-bromo-1-(4-(methylsulfonyl)phenyl)ethanone (Step 1) (60 g, 216 mmol, 1.075 eq.) in acetonitrile (630 mL) at 25° C. was added slowly Et 3 N (30.8 mL, 1.1 eq.). The mixture was stirred for 20 min. at r.t. and then cooled in an ice bath. DBU (60.1 mL, 3 eq.) was slowly added. After stirring for 20 min. in the ice bath, the reaction was complete and the mixture was acidified with 1N HCl (color changed from dark brown to yellow).
  • the solution is then diluted with 50 mL of benzene and washed with brine and 1N HCl.
  • the benzene solution is dried over Na 2 SO 4 , and concentrated.
  • the crude products are separated by column chromatography on silica gel, eluting with 2:1 EtOAc/hexane to give the title compound and its regioisomer.
  • reaction mixture is then treated with 2 mL of Et 3 N and 50 mL of sat. NaHCO 3 , and extracted with 100 mL of Et 2 O.
  • Et 2 O layer is dried over Na 2 SO 4 and concentrated to give the crude title compound which is used for the next step without further purification.
  • MMPP magnesium monoperoxyphthalate

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  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Psychiatry (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Furan Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
US09/180,647 1996-05-17 1997-05-13 Compositions for a once day treatment of cyclooxygenase-2 mediated diseases Expired - Lifetime US6063811A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US09/180,647 US6063811A (en) 1996-05-17 1997-05-13 Compositions for a once day treatment of cyclooxygenase-2 mediated diseases

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US1787896P 1996-05-17 1996-05-17
GB9612063 1996-06-10
GBGB9612063.9A GB9612063D0 (en) 1996-06-10 1996-06-10 Compositions for a once a day treatment of cyclooxygenase-2 mediated diseases
US85175697A 1997-05-06 1997-05-06
PCT/US1997/008041 WO1997044028A1 (fr) 1996-05-17 1997-05-13 Compositions pour traitement journalier monodose de maladies a mediateur cyclooxygenase-2
US09/180,647 US6063811A (en) 1996-05-17 1997-05-13 Compositions for a once day treatment of cyclooxygenase-2 mediated diseases

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US85175697A Continuation 1996-05-17 1997-05-06

Publications (1)

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US6063811A true US6063811A (en) 2000-05-16

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US09/180,647 Expired - Lifetime US6063811A (en) 1996-05-17 1997-05-13 Compositions for a once day treatment of cyclooxygenase-2 mediated diseases

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US (1) US6063811A (fr)
EP (1) EP0910368A1 (fr)
JP (1) JPH11512754A (fr)
KR (1) KR100373622B1 (fr)
CN (1) CN1140267C (fr)
AR (1) AR012014A1 (fr)
AU (1) AU3004997A (fr)
BG (1) BG103000A (fr)
BR (1) BR9709097A (fr)
CA (1) CA2254061C (fr)
CO (1) CO5050370A1 (fr)
CZ (1) CZ291463B6 (fr)
DZ (1) DZ2200A1 (fr)
EA (1) EA001596B1 (fr)
EE (1) EE03746B1 (fr)
HR (1) HRP970262A2 (fr)
HU (1) HUP9902889A3 (fr)
ID (1) ID16921A (fr)
IL (1) IL126899A (fr)
IS (1) IS4891A (fr)
MY (1) MY116201A (fr)
NO (1) NO985342D0 (fr)
NZ (1) NZ332670A (fr)
PE (1) PE66998A1 (fr)
PL (1) PL188649B1 (fr)
SK (1) SK284330B6 (fr)
TR (1) TR199802345T2 (fr)
WO (1) WO1997044028A1 (fr)

Cited By (11)

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US6476042B1 (en) 1999-06-30 2002-11-05 Pfizer Inc. Combination therapy for the treatment of migraine
US6511968B1 (en) * 1998-03-13 2003-01-28 Merck & Co., Inc. Combination therapy for treating, preventing, or reducing the risks associated with acute coronary ischemic syndrome and related conditions
US20030171437A1 (en) * 2002-03-07 2003-09-11 Jurij Holinej Pharmaceutical composition
US20030212050A1 (en) * 2000-08-29 2003-11-13 Peter Van Patten Prophylactic treatment of migraine
US20040132780A1 (en) * 2001-05-04 2004-07-08 Allen Christopher P. Method and compositions for treating migraines
US20100111858A1 (en) * 2007-01-19 2010-05-06 Howard Carol P Diangostic and Therapeutic Cyclooxygenase-2 Binding Ligands
US20150011514A1 (en) * 1998-11-30 2015-01-08 Pfizer Inc. Celecoxib Compositions
WO2020210341A1 (fr) * 2019-04-09 2020-10-15 Tremeau Pharmaceuticals, Inc. Traitement de fièvres hémorragiques virales avec des médicaments anti-inflammatoires non stéroïdiens sélectifs de cox-2
US10945992B1 (en) 2019-11-13 2021-03-16 Tremeau Pharmaceuticals, Inc. Dosage forms of rofecoxib and related methods
US10987337B2 (en) 2018-11-21 2021-04-27 Tremeau Pharmaceuticals, Inc. Purified forms of rofecoxib, methods of manufacture and use
US11858909B2 (en) 2021-04-09 2024-01-02 Tremeau Pharmaceuticals, Inc. Deuterated etoricoxib, methods of manufacture, and use thereof

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JP2002506024A (ja) * 1998-03-13 2002-02-26 メルク エンド カムパニー インコーポレーテッド 急性冠動脈虚血症候群および関連状態に対する併用療法および組成物
GB9920558D0 (en) * 1999-08-31 1999-11-03 Bradford Particle Design Ltd Methods for particle formation and their products
US20020015735A1 (en) * 1999-12-22 2002-02-07 Hedden David B. Sustained-release formulation of a cyclooxygenase-2 inhibitor
CA2411960C (fr) 2000-06-13 2010-10-12 Wyeth Compositions analgesiques et anti-inflammatoires contenant des inhibiteurs de cox-2
CN1638739A (zh) * 2000-08-18 2005-07-13 法玛西雅厄普约翰美国公司 治疗成瘾性障碍的化合物
DE60120710T2 (de) * 2000-08-18 2007-06-14 Pharmacia Corp. Schnell zerfallende orale arzneizubereitung enthaltend valdecoxib
AR030630A1 (es) * 2000-09-11 2003-08-27 Novartis Ag Composiciones farmaceuticas
US7115565B2 (en) * 2001-01-18 2006-10-03 Pharmacia & Upjohn Company Chemotherapeutic microemulsion compositions of paclitaxel with improved oral bioavailability
US20030114527A1 (en) * 2001-08-31 2003-06-19 Karnachi Anees Abdulquadar Pharmaceutical composition
CA2461044A1 (fr) * 2001-09-26 2003-04-03 Pharmacia Corporation Compositions de valdecoxib se desintegrant dans la bouche
HUP0401776A2 (hu) * 2001-10-10 2004-12-28 Pharmacia Corporation Intraorálisan széteső valdekoxib készítmények porlasztásos szárítási eljárással előállítva
ES2213485B1 (es) 2003-02-13 2005-12-16 Almirall Prodesfarma, S.A. Derivados de la 2-fenilpiran-4-ona.
ES2214129B1 (es) * 2003-02-13 2005-12-01 Almirall Prodesfarma, S.A. 3-fenilfuran-2-onas.
PL2266585T3 (pl) 2003-05-07 2013-10-31 Osteologix As Rozpuszczalne w wodzie sole stronktu do stosowania w leczeniu chorób chrząstki i/lub kości
TR200301552A1 (tr) * 2003-09-18 2005-10-21 Nobel İlaç Sanayi̇ Ve Ti̇caret A. Ş. Rofekoksib' in yeni oral farmakolojik formülasyonları.

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US20150011514A1 (en) * 1998-11-30 2015-01-08 Pfizer Inc. Celecoxib Compositions
US6476042B1 (en) 1999-06-30 2002-11-05 Pfizer Inc. Combination therapy for the treatment of migraine
US8680081B2 (en) 2000-08-29 2014-03-25 Peter Van Patten Prophylactic treatment of migraine
US20030212050A1 (en) * 2000-08-29 2003-11-13 Peter Van Patten Prophylactic treatment of migraine
US20040132780A1 (en) * 2001-05-04 2004-07-08 Allen Christopher P. Method and compositions for treating migraines
US20050123604A1 (en) * 2002-03-07 2005-06-09 Karnachi Anees A. Pharmaceutical compositions
US20090149543A1 (en) * 2002-03-07 2009-06-11 Anees Abdulquadar Karnachi Solid pharmaceutical compositions comprising lumiracoxib
US20070087051A1 (en) * 2002-03-07 2007-04-19 Jurij Holinej Pharmaceutical composition
US20030171437A1 (en) * 2002-03-07 2003-09-11 Jurij Holinej Pharmaceutical composition
US20100111858A1 (en) * 2007-01-19 2010-05-06 Howard Carol P Diangostic and Therapeutic Cyclooxygenase-2 Binding Ligands
US10987337B2 (en) 2018-11-21 2021-04-27 Tremeau Pharmaceuticals, Inc. Purified forms of rofecoxib, methods of manufacture and use
US11559509B2 (en) 2018-11-21 2023-01-24 Tremeau Pharmaceuticals, Inc. Purified forms of rofecoxib, methods of manufacture and use
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US11872206B2 (en) 2018-11-21 2024-01-16 Tremeau Pharmaceuticals, Inc. Purified forms of rofecoxib, methods of manufacture and use
WO2020210341A1 (fr) * 2019-04-09 2020-10-15 Tremeau Pharmaceuticals, Inc. Traitement de fièvres hémorragiques virales avec des médicaments anti-inflammatoires non stéroïdiens sélectifs de cox-2
US10945992B1 (en) 2019-11-13 2021-03-16 Tremeau Pharmaceuticals, Inc. Dosage forms of rofecoxib and related methods
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EA199801017A1 (ru) 1999-04-29
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BR9709097A (pt) 1999-08-03
HUP9902889A3 (en) 2002-04-29
SK284330B6 (sk) 2005-01-03
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HUP9902889A2 (hu) 2002-01-28
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